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Visual barcodes for clonal-multiplexing of live microscopy-based assays.

Kaufman T, Nitzan E, Firestein N, Ginzberg MB, Iyengar S, Patel N, Ben-Hamo R, Porat Z, Hunter J, Hilfinger A, Rotter V, Kafri R, Straussman R
Nat Commun. 2022 May 18;13(1):2725. doi: 10.1038/s41467-022-30008-0. (Link opens in a new window) PubMed (Link opens in a new window) Article

Plasmids from Article

ID Plasmid Purpose
158665Barcode backboneThis plasmid serves as the backbone for the visual barcodes described in our paper. It has a CMV-Puro-F2A backbone to which we insert a fluorescent protein cellular localization combination
158666mTAGBFP2 WC visual barcodetagging clonal populations with whole cell mTAGBFP2 fluorescent protein
158667mTAGBFP2 NES visual barcodetagging clonal populations with NES mTAGBFP2 fluorescent protein. Adding NES to mTAGBFP2 WC
158668mTAGBFP2 Peroxisome visual barcodetagging clonal populations with Peroxisomal mTAGBFP2 fluorescent protein. Adding Peroxisome localization signal to mTAGBFP2 WC
158669mTurquoise2 WC visual barcodetagging clonal populations with whole cell mTurquoise2 fluorescent protein
158670mTurquoise2 NES visual barcodetagging clonal populations with NES mTurquoise2 fluorescent protein.
158671mTurquoise2 Peroxisome visual barcodetagging clonal populations with Peroxisomal mTurquoise2 fluorescent protein.
158672acGFP WC visual barcodetagging clonal populations with whole cell acGFP fluorescent protein
158673acGFP NES visual barcodetagging clonal populations with NES acGFP fluorescent protein. Adding NES to acGFP WC
158674acGFP Peroxisome visual barcodetagging clonal populations with Peroxisomal acGFP fluorescent protein. Adding Peroxisome localization signal to acGFP WC
158675EYFP WC visual barcodetagging clonal populations with whole cell EYFP fluorescent protein
158676EYFP NES visual barcodetagging clonal populations with NES EYFP fluorescent protein. Adding NES to EYFP WC
158677EYFP Peroxisome visual barcodetagging clonal populations with Peroxisomal EYFP fluorescent protein. Adding Peroxisome localization signal to EYFP WC
158678TRE reporter backboneThis plasmid serves as the backbone for the TRE reporters described in our paper. It's a promoterless-mStrawberry-pGK-BSD backbone to which we insert a pathway specific promoter before the mStrawberry
158681HIF-TRE-mStrawberry reporterThis plasmid is a HIF1A pathway reporter. It has a 6 x HIF binding element promoter driving the expression of mStrawberry-pGK-BSD
158682YAP/TAZ-TRE-mStrawberry reporterThis plasmid is a YAP/TAZ pathway reporter. It has a YAP/TAZ-responsive synthetic promoter driving the expression of mStrawberry-pGK-BSD
158683RAR-TRE-mStrawberry reporterThis plasmid is a RAR pathway reporter. It has a Retinoic Acid Receptor Response Element promoter driving the expression of mStrawberry-pGK-BSD
158684p53-TRE-mStrawberry reporterThis plasmid is a p53 pathway reporter. It has two copies of wild-type p53 binding sites promoter driving the expression of mStrawberry-pGK-BSD
158685AKT-translocation-mStrawberry reporterThis plasmid is a AKT pathway reporter. It has 1EF1a promoter driving the expression of truncated FoxO1 fused to mStrawberry-pGK-BSD
158686ERK-KTR-mStrawberry reporterThis plasmid is a ERK pathway reporter. It has CMV promoter driving the expression of ERK-KTR fused to mStrawberry-pGK-BSD
158687p38-KTR-mStrawberry reporterThis plasmid is a p38 pathway reporter. It has CMV promoter driving the expression of p38-KTR fused to mStrawberry-pGK-BSD
158688PKA-KTR-mStrawberry reporterThis plasmid is a PKA pathway reporter. It has CMV promoter driving the expression of PKA-KTR fused to mStrawberry-pGK-BSD
158689JNK-KTR-mStrawberry reporterThis plasmid is a JNK pathway reporter. It has CMV promoter driving the expression of JNK-KTR fused to mStrawberry-pGK-BSD
158690Geminin-mStrawberry reporterThis plasmid is a Geminin cell cycle reporter. It has CMV promoter driving the expression of Geminin fused to mStrawberry-pGK-BSD
158691iRFP-H2AThis plasmid encodes an iRFP fused to H2A histone nuclear marker. It has CMV promoter driving the expression of iRFP fused to H2A. It has no selection markers

Antibodies from Article